WO2020262730A1 - Fil d'acier plaqué et son procédé de fabrication - Google Patents

Fil d'acier plaqué et son procédé de fabrication Download PDF

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Publication number
WO2020262730A1
WO2020262730A1 PCT/KR2019/007726 KR2019007726W WO2020262730A1 WO 2020262730 A1 WO2020262730 A1 WO 2020262730A1 KR 2019007726 W KR2019007726 W KR 2019007726W WO 2020262730 A1 WO2020262730 A1 WO 2020262730A1
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WO
WIPO (PCT)
Prior art keywords
steel wire
zinc alloy
alloy plating
plating layer
plated steel
Prior art date
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PCT/KR2019/007726
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English (en)
Korean (ko)
Inventor
김태철
김종성
강성훈
유광원
손일령
김종상
Original Assignee
주식회사 포스코
고려제강 주식회사
홍덕산업 주식회사
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Application filed by 주식회사 포스코, 고려제강 주식회사, 홍덕산업 주식회사 filed Critical 주식회사 포스코
Priority to JP2021577188A priority Critical patent/JP7290757B2/ja
Priority to EP19935169.3A priority patent/EP3992326A4/fr
Priority to US17/622,085 priority patent/US11834747B2/en
Priority to CN201980097811.9A priority patent/CN114072533A/zh
Priority to MYPI2021007737A priority patent/MY197182A/en
Priority to PCT/KR2019/007726 priority patent/WO2020262730A1/fr
Publication of WO2020262730A1 publication Critical patent/WO2020262730A1/fr
Priority to US18/519,969 priority patent/US20240093341A1/en

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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/06Zinc or cadmium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C18/00Alloys based on zinc
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C18/00Alloys based on zinc
    • C22C18/04Alloys based on zinc with aluminium as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • C23C2/024Pretreatment of the material to be coated, e.g. for coating on selected surface areas by cleaning or etching
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/34Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
    • C23C2/36Elongated material
    • C23C2/38Wires; Tubes
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/02Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material
    • C23C28/023Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material only coatings of metal elements only
    • C23C28/025Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material only coatings of metal elements only with at least one zinc-based layer

Definitions

  • the present invention relates to a plated steel wire and a method of manufacturing the same, and more particularly, to a plated steel wire having effective workability and corrosion resistance, and a method of manufacturing the same.
  • the galvanizing method is widely used to manufacture steel materials having high corrosion resistance due to its excellent anticorrosive performance and economy.
  • the hot-dip galvanized steel which forms a plating layer by immersing the steel in a hot-dip galvanizing bath, has a simpler manufacturing process and a low product price compared to the electro-galvanized steel, so its demand is increasing in various fields.
  • Hot-dip galvanized steel with a galvanized layer has the characteristics of sacrificial corrosion protection in which Zn, which has a lower oxidation-reduction potential than Fe, is first corroded when exposed to a corrosive environment, thereby inhibiting the corrosion of the steel.
  • Zn which has a lower oxidation-reduction potential than Fe
  • the steel material is blocked from the oxidizing atmosphere by forming a dense corrosion product on the steel material surface, so that the corrosion resistance of the steel material can be effectively improved.
  • Zn-Al alloy plated steel wire has been developed to meet these needs.
  • Zn-Al alloy-plated steel wire is generally subjected to a flux treatment to activate an interfacial reaction with zinc after cleaning operations such as pickling, washing, and degreasing, and can be manufactured by immersing in a Zn-based plating bath containing Al.
  • Patent Document Republic of Korea Patent Publication No. 10-2016-0078670 (published on May 5, 2016)
  • a plated steel wire and a method of manufacturing the same, which effectively secures workability and corrosion resistance.
  • the plated steel wire according to an aspect of the present invention includes a base steel wire and a zinc alloy plated layer, and the zinc alloy plated layer is, by weight, Al: 1.0 to 3.0%, Mg: 1.0 to 2.0%, Fe: 0.5 to 5.0 %, including the remaining Zn and inevitable impurities, including a Zn/MgZn 2 /Al ternary process structure, a Zn single phase structure, and a Fe-Zn-Al-based crystal structure, and the Fe-Zn-Al-based crystal structure It is formed adjacent to the steel wire, and may have an average thickness of 1/5 to 1/2 of the average thickness of the zinc alloy plating layer.
  • the area fraction occupied by the Zn single-phase structure may be 60% or more.
  • the average spacing of columnar crystals of the single-phase Zn structure in the cross section of the zinc alloy plating layer may be 1 to 5 ⁇ m.
  • a method of manufacturing a plated steel wire includes providing a galvanized steel wire by first immersing a holding steel wire in a hot-dip galvanizing bath; Providing a zinc-alloy-plated steel wire by second immersing the first immersed galvanized steel wire in a hot-dip zinc alloy plating bath; The second immersed zinc alloy plated steel wire is cooled at a cooling rate of 15 to 50°C/s, but the molten zinc alloy plating bath is, by weight, Al: 1.0 to 3.0%, Mg: 1.0 to 2.0%, the rest It may contain Zn and unavoidable impurities.
  • the holding steel wire may be first immersed for 10 to 20 seconds in the molten zinc plating bath at 440 to 460°C.
  • the first immersed galvanized steel wire may be cooled to a temperature range equal to or lower than the melting point of Zn, and then second immersed in the molten zinc alloy plating bath.
  • the galvanized steel wire may be secondarily immersed in the molten zinc alloy plating bath at 440 to 460°C for 10 to 20 seconds.
  • a plated steel wire and a method for manufacturing the same according to an aspect of the present invention can provide a plated steel wire and a method for manufacturing the same, which have effectively improved workability and corrosion resistance.
  • Example 1 is an FE-SEM image observing a cross section of Inventive Example 1.
  • Example 5 is a SEM image of the surface of Inventive Example 1 after drawing.
  • the present invention relates to a plated steel wire and a method of manufacturing the same.
  • preferred embodiments of the present invention will be described.
  • the embodiments of the present invention may be modified in various forms, and the scope of the present invention should not be construed as being limited to the embodiments described below.
  • the present embodiments are provided to explain the present invention in more detail to those of ordinary skill in the art to which the present invention pertains.
  • the plated steel wire according to an aspect of the present invention may include a holding steel wire and a zinc alloy plating layer.
  • the holding steel wire of the present invention is not limited to a specific type of steel wire, and may be interpreted as including all kinds of steel wires used for hot-dip galvanizing or hot-dip galvanizing.
  • the zinc alloy plating layer of the plated steel wire according to an aspect of the present invention contains Al: 1.0 to 3.0%, Mg: 1.0 to 2.0%, Fe: 0.5 to 5.0%, the remaining Zn and unavoidable impurities. I can.
  • the composition of the zinc alloy plating layer of the present invention will be described in more detail.
  • the% related to the content of the alloy composition means% by weight.
  • Mg is an element that plays a very important role in improving the corrosion resistance of the zinc alloy plating layer.
  • Mg is contained in the zinc alloy plating layer, so it can suppress the generation of zinc oxide-based corrosion products that have little effect of improving corrosion resistance in severe corrosive environments, and stabilize zinc hydroxide-based corrosion products that are dense and have a high corrosion resistance improvement effect on the surface of the plating layer. . Therefore, in order to achieve this effect, the Mg content of the present invention may be 1.0% or more. However, when the content of Mn is excessively added, the effect of improving corrosion resistance due to the addition of Mg is saturated, and the oxidizing dross formed by the oxidation of Mg increases rapidly at the liquid level of the molten zinc alloy plating bath.
  • the Mg content of the present invention may be 2.0% or less.
  • Al is an element added to reduce dross caused by the oxidation reaction of Mg in the molten zinc alloy plating bath to which Mg is added.
  • Al is an element capable of improving the corrosion resistance of a plated steel wire in combination with Zn and Mg. Therefore, in order to achieve this effect, the Al content of the present invention may be 1.0% or more.
  • the preferred Al content may be at least 1.5%.
  • the Al content is excessively added, the elution amount of Fe of the steel wire immersed in the molten zinc alloy plating bath increases rapidly, thereby forming an Fe alloy dross.
  • the Al-Zn metal structure is formed in the hot-dip zinc alloy plating bath, so that the temperature of the plating bath increases, and the Al-Zn metal structure formed in the zinc alloy plating layer may impair the workability of the zinc alloy plating layer. Therefore, the Al content of the present invention may be 3.0% or less. The preferred Al content may be 2.8% or less.
  • Fe contained in the zinc alloy plating layer of the present invention is an element introduced into the zinc alloy plating layer by reacting Fe in the base steel sheet with Zn in the molten zinc alloy plating bath to form Fe-Zn.
  • the present invention is to secure the adhesion of the plating layer by forming a Fe-Zn-Al-based crystal structure at the interface of the zinc alloy plating layer, the Fe content contained in the zinc alloy plating layer of the present invention may be 0.5% or more, preferred Fe The content may be 0.8% or more.
  • the Fe content contained in the zinc alloy plating layer of the present invention may be 5.0% or less, and the preferred Fe content may be 4.3% or less.
  • the zinc alloy plating layer of the present invention may contain the remaining Zn and other unavoidable impurities.
  • Unintended impurities may inevitably be mixed from raw materials or the surrounding environment in the normal steel manufacturing process, and this cannot be completely excluded. Since these impurities are known to anyone of ordinary skill in the steel manufacturing process, all the contents are not specifically mentioned in the present invention.
  • the zinc alloy plating layer of the present invention may include a Zn/MgZn 2 /Al ternary process structure, a Zn single-phase structure, and a Fe-Zn-Al-based crystal structure.
  • the Fe-Zn-Al-based crystal structure is formed adjacent to the holding steel wire, and may be formed to have an average thickness of 1/5 to 1/2 of the average thickness of the zinc alloy plating layer.
  • the Fe-Zn-Al-based crystal structure is formed from the interface with the holding steel wire to a region of 1/5 to 1/2 thickness of the average thickness of the zinc alloy plated layer, so the adhesion between the zinc alloy plated layer and the holding steel wire It can be secured effectively. Accordingly, the occurrence of cracks in the zinc alloy plating layer or peeling of the zinc alloy plating layer can be effectively prevented during processing of the plated steel wire of the present invention, and the plated steel wire of the present invention can secure excellent workability.
  • the area fraction occupied by the Zn single-phase structure may be 60% or more, and the area fraction of the preferred Zn single-phase structure is 60-90 It can be %.
  • the average spacing of the Zn single-phase structured columnar crystals can be uniformly distributed at a level of 1 to 5 ⁇ m, and accordingly, the Zn/MgZn 2 /Al ternary process structure can be evenly distributed between the Zn single-phase structures.
  • the zinc alloy plating layer of the present invention includes a uniform Zn single-phase structure and a Zn/MgZn 2 /Al ternary process structure, and may have uniform corrosion resistance.
  • a method of manufacturing a plated steel wire according to an aspect of the present invention includes providing a galvanized steel wire by first immersing a holding steel wire in a hot-dip galvanizing bath; Providing a zinc-alloy-plated steel wire by second immersing the first immersed galvanized steel wire in a hot-dip zinc alloy plating bath; The second immersed zinc alloy-plated steel wire may be cooled at a cooling rate of 15 to 50°C/s.
  • the hot-dip galvanizing bath of the present invention refers to a plating bath in which Zn is the main component, but may contain impurities that are unavoidably introduced in the plating bath manufacturing process.
  • the hot-dip galvanizing bath of the present invention may mean a plating bath close to pure Zn in which a large amount of alloy components such as Al and Mg are not artificially added. Accordingly, the hot-dip galvanizing bath of the present invention may contain 95% or more Zn, preferably 98% or more Zn, and more preferably 99% or more Zn.
  • the composition content of the molten zinc alloy plating bath of the present invention corresponds to the reason for limiting the composition content of the zinc alloy plating layer described above, and the explanation of the reason for limiting the composition content of the molten zinc alloy plating bath of the present invention is described above. It replaces with the explanation of the reason for limiting the compositional content of the plating layer.
  • the Fe component of the zinc alloy plating layer is a component introduced from the holding steel wire
  • the description related to the Fe component in the above description of the composition content of the zinc alloy plating layer is in the description of the composition content of the molten zinc alloy plating bath of the present invention. Can be excluded.
  • the base steel wire can be cleaned by processes such as pickling, washing and degreasing, and a flux treatment can be performed.
  • a galvanized steel wire can be manufactured by first immersing the base steel wire through this pretreatment process in a hot dip galvanizing bath at 440 to 460°C for 10 to 20 seconds. Accordingly, a zinc-plated layer of Zn as a main component may be formed on the galvanized steel wire that is first immersed.
  • Zn-Al-Mg-containing composite ingot or Zn-Mg Zn-Al ingot containing individual components, in weight percent, Al: 1.0-3.0%, Mg: 1.0-2.0%, remaining Zn and inevitable
  • a molten zinc alloy bath containing impurities can be prepared.
  • a suitable temperature range for melting these ingots may be 440 to 520°C. The higher the melting temperature of the ingot, the more fluidity and uniform composition in the plating bath can be secured, and the amount of floating dross can be reduced. Thus, the ingot can be melted by heating in a temperature range of 440°C or higher.
  • the temperature of the molten zinc alloy plating bath exceeds 520°C, it is highly likely that ash-like surface defects may occur due to the evaporation of Zn, so it is preferable to limit the melting temperature of the ingot to 520°C or less. .
  • the melting of the molten zinc alloy plating bath is stabilized in the temperature range of 440 to 480°C. It is desirable to complete.
  • the first immersed galvanized steel wire can be cooled to a temperature range below the melting point of Zn, and then immersed in a molten zinc alloy plating bath prepared through the above-described process.
  • the temperature of the hot-dip zinc alloy plating bath provided for the secondary immersion may be applied to a conventional plating bath temperature, preferably in a temperature range of 440 to 480°C.
  • the second immersion time may also be appropriately applied in consideration of the thickness of the zinc alloy plating layer, and preferably, the second immersion may be performed for 10 to 20 seconds.
  • the galvanized layer formed on the surface of the holding steel sheet by the first immersion can be partially or completely dissolved again during the second immersion, and at this time, the Al component contained in the zinc alloy plating solution can diffuse and move toward the interface side with the holding steel sheet.
  • the zinc-alloy-plated steel wire after secondary immersion can be cooled at a cooling rate of 15 to 50°C/s, and preferably, the zinc alloy-plated steel wire is cooled at a cooling rate of 15 to 50°C/s immediately after the second immersion is completed. Can cool. That is, cooling can be started from the hot water surface of the molten zinc alloy plating bath.
  • the cooling rate of the present invention may be 15°C/s or more.
  • the Zn single-phase structured columnarity is excessively coarse, and uniform corrosion resistance cannot be ensured.
  • the Zn/MgZn 2 binary process structure formed in the plating layer causes cracks during processing of the coated steel wire, uniform corrosion resistance and workability may be impaired.
  • the cooling rate is excessive, the columnar crystals of the Zn single-phase structure may be excessively refined, resulting in locally uneven corrosion resistance, and the diffusion of the Fe-Zn-Al-based structure is insufficient, and the crystal structure is concentrated in the interface layer. As it is formed, a sufficient bonding force between the hot-dip galvanized layer and the steel wire cannot be expected, and thus the workability of the coated steel wire may be inferior.
  • Cooling of the present invention may be carried out by supplying an inert gas such as nitrogen, argon, and helium, but relatively inexpensive nitrogen may be preferable in terms of manufacturing cost reduction.
  • an inert gas such as nitrogen, argon, and helium
  • a plating steel wire was manufactured by applying different cooling conditions. .
  • the area ratio of the single-phase Zn structure refers to the ratio of the area occupied by the single-phase Zn-phase structure among the areas occupied by the single-phase Zn structure and the ternary process structure of Zn/MgZn 2 /Al in the cross section of the plating layer.
  • each plated steel wire was drawn at a diameter reduction rate of 80% and processed into 1mm plated steel wire, and the surface appearance and corrosion resistance of the processed plated steel wire were evaluated.
  • the surface appearance evaluation was performed by photographing the surface of the drawn plated steel sheet using SEM, and it was determined based on the presence or absence of cracks in the image.
  • Corrosion resistance was evaluated by performing a salt spray test on each of the drawn steel wires. That is, after each plated steel wire was loaded into a salt spray tester, the red rust generation time was measured according to the international standard (ASTM B117-11).
  • a 5% concentration of brine (temperature: 35°C, pH 6.8) was sprayed at an injection amount of 2ml/80cm 2 per hour.
  • the red rust generation time is 300 hours or more, " ⁇ ", 200 hours or more and less than 300 hours, " ⁇ ", 100 hours or more and less than 200 hours, " ⁇ ", and "X" when less than 100 hours.
  • the red rust generation time is more than 300 hours, it means that excellent corrosion resistance can be secured even in a severe oxidizing environment.
  • Inventive Examples 1 to 4 satisfies the conditions of the present invention, and it can be seen that cracks did not occur after drawing, and red rust was generated after 300 hours elapsed in the salt spray evaluation. On the other hand, Inventive Examples 1 to 4 did not satisfy the conditions of the present invention, and cracks occurred after drawing, and it was confirmed that red rust occurred within 200 hours when the salt spray was evaluated.
  • FIG. 1 is an FE-SEM image observing a cross section of Inventive Example 1
  • FIG. 2 is an FE-SEM image observing the surface of a plating layer of Inventive Example 1.
  • the area fraction of the single-phase Zn structure is about 85%, and the average spacing of the columnar crystals of the single-phase Zn structure is 3 ⁇ m, and the columnar crystals of the single-phase Zn structure are fine. It can be confirmed that it was formed.
  • the Fe-Zn-Al-based crystal structure was formed at a level of about 1/5 from the interface with respect to the total plating layer thickness, and the Zn/MgZn 2 /Al ternary process structure was evenly distributed between the Zn single-phase structures. It can be confirmed that it is distributed.
  • FIG. 3 is an FE-SEM image observing the cross section of Comparative Example 1
  • FIG. 4 is an FE-SEM image observing the surface of the plating layer of Comparative Example 1.
  • the area fraction of the single-phase Zn structure is about 50%, and the average spacing of the columnar crystals of the single-phase Zn structure is at the level of 15 ⁇ m, and the columnar crystals of the single-phase Zn structure are coarse. It can be confirmed that it was formed.
  • the Fe-Zn-Al-based crystal structure is a thin layer was formed to about 1/6 the level, Zn / MgZn 2 ternary 2 coarse tissue incorporation process from the interface over the entire thickness of the coating layer, a whole tissue It can be seen that it is distributed unevenly.
  • FIG. 5 is an SEM image of the surface after drawing of Inventive Example 1
  • FIG. 6 is an SEM image of the surface of Comparative Example 1 after drawing.
  • a plated steel wire and a method for manufacturing the same can provide a plated steel wire and a method for manufacturing the same, effectively securing workability and corrosion resistance.

Abstract

Un fil d'acier plaqué, selon un aspect de la présente invention, comprend : un fil d'acier de base ; et une couche plaquée d'alliage de zinc. La couche plaquée d'alliage de zinc comprend, en pourcentage en poids : 1,0 % à 3,0 % d'AI ; 1,0 % à 2,0 % de Mg ; 0,5 % à 5,0 % de Fe ; et le reste étant du Zn et des impuretés inévitables, et comprend une structure eutectique ternaire Zn/MgZn2/AI, une structure à phase unique de Zn, et une structure cristalline à base de Fe-Zn-AI, la structure cristalline à base de Fe-Zn-AI étant formée adjacente au fil d'acier de base, et pouvant avoir une épaisseur moyenne de 1/5 à 1/2 par rapport à une épaisseur moyenne de la couche plaquée d'alliage de zinc.
PCT/KR2019/007726 2019-06-26 2019-06-26 Fil d'acier plaqué et son procédé de fabrication WO2020262730A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP2021577188A JP7290757B2 (ja) 2019-06-26 2019-06-26 めっき鋼線及びその製造方法
EP19935169.3A EP3992326A4 (fr) 2019-06-26 2019-06-26 Fil d'acier plaqué et son procédé de fabrication
US17/622,085 US11834747B2 (en) 2019-06-26 2019-06-26 Plated steel wire and manufacturing method for the same
CN201980097811.9A CN114072533A (zh) 2019-06-26 2019-06-26 镀覆钢丝及其制造方法
MYPI2021007737A MY197182A (en) 2019-06-26 2019-06-26 Plated steel wire and manufacturing method for the same
PCT/KR2019/007726 WO2020262730A1 (fr) 2019-06-26 2019-06-26 Fil d'acier plaqué et son procédé de fabrication
US18/519,969 US20240093341A1 (en) 2019-06-26 2023-11-27 Plated steel wire and manufacturing method for the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/KR2019/007726 WO2020262730A1 (fr) 2019-06-26 2019-06-26 Fil d'acier plaqué et son procédé de fabrication

Related Child Applications (2)

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US17/622,085 A-371-Of-International US11834747B2 (en) 2019-06-26 2019-06-26 Plated steel wire and manufacturing method for the same
US18/519,969 Division US20240093341A1 (en) 2019-06-26 2023-11-27 Plated steel wire and manufacturing method for the same

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WO2020262730A1 true WO2020262730A1 (fr) 2020-12-30

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US (2) US11834747B2 (fr)
EP (1) EP3992326A4 (fr)
JP (1) JP7290757B2 (fr)
CN (1) CN114072533A (fr)
MY (1) MY197182A (fr)
WO (1) WO2020262730A1 (fr)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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